ea0041oc5.3 | Neuroendocrinology | ECE2016
Wilkinson Ian
, Pradhananga Sarbendra
, Speak Rowena
, Sayers Jon
, Ross Richard
Background: The UK acromegaly register reported that <60% of acromegalics on medical therapy had controlled disease (1). Pegvisomant, a growth hormone antagonist (GHA), controls disease in >95% cases, but is not cost-effective and requires high dose daily injections (2). We have developed a fusion technology for making a cost-effective long-acting GH molecule (3), and generated a GHA by linking mutated growth hormone to its binding protein (GHBP).<p class="abstext"...